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Medtronic Sofamor Danek USA, Incorporated

FDA Regulatory Profile

Medtronic Sofamor Danek USA, Incorporated appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 6, 2016.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K152604KYPHON HV-R Fenestrated Screw Cement, CD HORIZON Fenestrated Screw SetJanuary 6, 2016
K150200CD HORIZON Growth Rod Conversion SetFebruary 25, 2015

FDA data resources